Variant report

Variant	rs7669132
Chromosome Location	chr4:95811312-95811313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:95678457..95680699-chr4:95808696..95811437,2	MCF-7	breast:
2	chr4:95810479..95814160-chr4:95814675..95817418,3	K562	blood:

Variant related genes	Relation type
ENSG00000138696	Chromatin interaction
ENSG00000249599	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10213566	1.00[CEU][hapmap]
rs11932204	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11932515	1.00[CEU][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11932610	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11935769	0.85[YRI][hapmap]
rs11936523	0.92[EUR][1000 genomes]
rs11941775	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11943147	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1541368	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1541370	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1541371	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022139	0.83[YRI][hapmap]
rs17022361	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022438	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022440	1.00[CEU][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs17022443	1.00[CEU][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs17022451	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022456	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs17022474	1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022484	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17022491	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022496	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17022509	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022514	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022528	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022567	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2865408	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56353739	0.92[EUR][1000 genomes]
rs57560594	0.92[EUR][1000 genomes]
rs58414599	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58554231	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61352548	0.81[AFR][1000 genomes]
rs6828737	0.92[EUR][1000 genomes]
rs6829384	0.92[EUR][1000 genomes]
rs6851515	0.92[EUR][1000 genomes]
rs6851550	0.92[EUR][1000 genomes]
rs6851705	0.92[EUR][1000 genomes]
rs72887844	0.92[EUR][1000 genomes]
rs72887846	0.92[EUR][1000 genomes]
rs73836127	0.92[EUR][1000 genomes]
rs73836128	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73836142	1.00[EUR][1000 genomes]
rs73836153	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73836154	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73836181	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73836183	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73836186	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73836191	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7661079	1.00[CEU][hapmap]
rs7669913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7669132	SCGB1D2	trans	brain	seeQTL
rs7669132	SCGB2A2	trans	brain	seeQTL

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95804000-95813200	Weak transcription	A549	lung
2	chr4:95809800-95811600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:95810400-95811600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:95810400-95813600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:95810600-95811400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:95810600-95811400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:95810600-95811400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:95810600-95811400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:95810600-95811600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:95810600-95811600	Enhancers	HMEC	breast
11	chr4:95810600-95811600	Enhancers	NH-A	brain
12	chr4:95810800-95811400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr4:95810800-95811400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:95810800-95811400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:95810800-95811400	Enhancers	Fetal Muscle Leg	muscle
16	chr4:95810800-95811400	Enhancers	Psoas Muscle	Psoas
17	chr4:95810800-95811400	Enhancers	NHEK	skin
18	chr4:95810800-95811600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:95811000-95811600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:95811000-95833600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:95811200-95811400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr4:95811200-95811800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:95811200-95815200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:95811200-95815400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:95811200-95817800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr4:95811200-95824800	Weak transcription	Aorta	Aorta

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